szx16 research stereo zoom microscope (Olympus)
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szx16 research stereo zoom microscope
Szx16 Research Stereo Zoom Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 96/100, based on 6427 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/stereo+microscope/SZX16+Research+Stereo+Microscope+System/pmc13692848-285-8-13
Average 96 stars, based on 6427 article reviews
Szx16 Research Stereo Zoom Microscope, supplied by Olympus, used in various techniques. Bioz Stars score: 96/100, based on 6427 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/stereo+microscope/SZX16+Research+Stereo+Microscope+System/pmc13692848-285-8-13
Average 96 stars, based on 6427 article reviews
szx16 research stereo zoom microscope - by Bioz Stars,
2026-11
96/100 stars
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Microscopy:Article Title: Visualizing the 3D morphological structure and dynamic defensive characteristics of teleost mucus barrier through an ex vivo approach in flounder (Paralichthys olivaceus). Article Snippet: The fish mucus barrier serves as the first line of defense against pathogen invasion, and its structural and functional changes are key indicators for assessing fish health.. However, due to limitations in situ observation techniques, the three-dimensional (3D) architecture and dynamic barrier functions of the fish mucus layer have long remained poorly understood.. 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![( A ) scRNA-seq workflow. Created in BioRender. Kadota, C. (2026) https://BioRender.com/ks47d2b . ( B ) UMAP visualization of cell types in TMJ. Chondrocytes are highlighted in blue. ( C ) Proportion of each cell cluster in p75 +/+ and p75 −/− MCCs. ( D ) Pathway analysis of chondrocytes identified by scRNA-seq. ( E ) <t>Stereomicroscope</t> images and gross pellet size. Scale bar, 500 μm. ( F ) Safranin O staining [Top: Whole-pellet view (10×; scale bar, 500 μm); bottom, 40× view of the dotted area. Scale bar, 100 μm] and quantification of Safranin O–positive area, and ( G ) gene expression analyses ( Acan , Ihh , Sox9 , and Col2a1 ) of p75 +/+ and p75 −/− mBMSCs underwent 3D pellet culture ( N = 6 per group). ( H ) Left: Western blotting of p75 NTR , phosphorylated-AKT, AKT, phosphorylated-p38, and p38 in mBMSCs treated with vehicle or BDNF. Right: Quantification of p-AKT/AKT and p-p38/p38 ratios. ( N = 5 independent experiments). ( I ) Gene expression analyses in p75 +/+ and p75 −/− condyles for p75 NTR , Ntrk2 , Bdnf , Trp53 , Bax , Acan , Ihh , Sox9 , Col2a1 , and Mki67 ( N = 5 per group). IF staining for ( J ) Ki-67 and ( K ) TUNEL and quantification of Ki-67 and TUNEL-positive cells in p75 +/+ and p75 −/− TMJ ( N = 5 per group). Blue, DAPI. Scale bar, 50 μm. ( L ) Cell proliferation assay of mBMSCs derived from p75 +/+ and p75 −/− mice ( N = 5 per group). ( M ) Apoptosis assay of mBMSCs derived from p75 +/+ and p75 −/− mice ( N = 5 per group). Statistical significance was determined using unpaired two-sided Student’s t test or two-way ANOVA, as appropriate. Bonferroni correction was applied for pairwise post hoc comparisons following two-way ANOVA. Results are represented as the means ± 1 SEM. * P < 0.05, ** P < 0.01, *** P < 0.001. N represents the number of mice or experimental replicates.](https://pub-med-central-images-cdn.bioz.com/pub_med_central_ids_ending_with_5922/pmc13685922/pmc13685922__sciadv.aef7786-f6.jpg)